Hepatoprotection by chemical constituents of the marine brown alga Spatoglossum variabile: a relation to free radical scavenging potential

Pharm Biol. 2013 Mar;51(3):383-90. doi: 10.3109/13880209.2012.732582.

Abstract

Context: In the course of searching hepatoprotective agents from natural sources, the protective effect of chemical constituents of the marine brown alga Spatoglossum variabile Figaro et DE Notar (Dictyoaceae) against CCl₄-induced liver damage in Wistar rats was investigated. The compounds were first investigated for in vitro radical scavenging potential and were also tested for β-glucuronidase inhibition to further explore the relationship between hepatoprotection and antiradical potential.

Methods: The compounds cinnamic acid esters 1 and 2 and aurone derivatives 3 and 4 were first investigated for in vitro radical scavenging potential against 1,1-diphenyl-2-picrylhydrazyl radicals (DPPH), and superoxide anion radicals. In vivo hepatoprotective studies were performed in seven groups (n = 6) of Wistar rats. The test groups were pretreated with compounds (10 mg/kg body weight, po) orally for 30 min before the intraperitoneal administration of a dose of 20% CCl₄ diluted with dietary cooking oil. Moreover, compounds were also tested for β-glucuronidase inhibition to explore the relationship between hepatoprotection and radical scavenging potential.

Results: The test compounds 1-4 were found to exhibit antiradical activity against 1,1-diphenyl-2-picrylhydrazyl radicals with IC₅₀ values ranging between 54 and 138 µM, whereas aurone derivatives 3 and 4 additionally exhibited superoxide anion scavenging effects with IC₅₀ values of 95 and 87 µM, respectively. In addition, these compounds were found to be weak inhibitors of xanthine oxidase (IC₅₀ ≥1000 µM). In animal model, pretreatment with compounds 2-4 significantly blocked the CCl₄-induced increase in the levels of the serum biochemical markers.

Conclusion: It appears that the hepatoprotection afforded by these compounds was mainly due to their radical scavenging activity that protected the cells from the free radicals generated by CCl₄-induced hepatotoxicity.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Benzofurans / adverse effects
  • Benzofurans / chemistry
  • Benzofurans / pharmacology
  • Benzofurans / therapeutic use*
  • Biomarkers / blood
  • Carbon Tetrachloride Poisoning / blood
  • Carbon Tetrachloride Poisoning / physiopathology
  • Carbon Tetrachloride Poisoning / prevention & control*
  • Cell Survival / drug effects
  • Cinnamates / adverse effects
  • Cinnamates / chemistry
  • Cinnamates / pharmacology
  • Cinnamates / therapeutic use*
  • Drug Discovery
  • Enzyme Inhibitors / adverse effects
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology
  • Enzyme Inhibitors / therapeutic use
  • Escherichia coli Proteins / antagonists & inhibitors
  • Free Radical Scavengers / adverse effects
  • Free Radical Scavengers / chemistry
  • Free Radical Scavengers / pharmacology
  • Free Radical Scavengers / therapeutic use*
  • Glucuronidase / antagonists & inhibitors
  • Humans
  • Liver / drug effects*
  • Liver / physiopathology
  • Male
  • Milk Proteins / antagonists & inhibitors
  • Neutrophils / drug effects
  • Phaeophyceae / chemistry*
  • Rats
  • Rats, Wistar
  • Xanthine Oxidase / antagonists & inhibitors

Substances

  • 4'-chloro-2-hydroxyaurone
  • 4'-chloroaurone
  • Benzofurans
  • Biomarkers
  • Cinnamates
  • Enzyme Inhibitors
  • Escherichia coli Proteins
  • Free Radical Scavengers
  • Milk Proteins
  • butyl-3,5-dimethoxy-4-hydroxycinnamate
  • isopropyl 3,5-dimethoxy-4-hydroxycinnamate
  • Xanthine Oxidase
  • Glucuronidase